510(k) K092746 ยท FMI Needle, Hypodermic, Single Lumen
MICRONJET 600
| Applicant | Nanopass Technologies , Ltd., Washington DC, US |
| Decision | Substantially Equivalent, Feb 3, 2010 |
| Received | Sep 8, 2009 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K092746
No recall in the FDA data names this 510(k).
Links come from the 510(k) numbers listed on each FDA recall record. We don't infer predicate chains.